FDA Device recall Z-1324-2017
Lap Band Pack, part number AMS1785(A
- FDA Device
- Class II
- terminated
- Published 2017-03-08
On 2017-03-08 the FDA classified a Class II recall of Lap Band Pack, part number AMS1785(A by Windstone Medical Packaging, citing the Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterili….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1324-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-11 |
| Published | 2017-03-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Windstone Medical Packaging |
| Distribution | AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, WA |
Product
Lap Band Pack, part number AMS1785(A
Reason
The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.
Identifiers
| code_info | Lot number and expiration date 85157, 2/28/2017 86861, 2/28/2017 87419, 4/30/2017 88367, 3/31/2017 89154, 7/31/2…Lot number and expiration date 85157, 2/28/2017 86861, 2/28/2017 87419, 4/30/2017 88367, 3/31/2017 89154, 7/31/2017 94568, 7/31/2017 94919, 11/30/2017 95972, 10/31/2017 96744, 11/30/2017 97772, 11/30/2017 98016, 11/30/2017 98495, 3/31/2018 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1324-2017%22
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